Canonical Allele Identifier: CA1435013391
Gene: MSX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.4862346T= , CM000666.2:g.4862346T= GRCh38
NC_000004.11:g.4864073T= , CM000666.1:g.4864073T= GRCh37
NC_000004.10:g.4914974T= NCBI36
NG_008121.1:g.7682T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382723.5:c.470-355T= MANE Select ENSP00000372170.4:n.470-355T=
ENST00000382723.4:c.470-355T= ENSP00000372170.4:n.470-355T=
NM_002448.3:c.470-355T= MANE Select NP_002439.2:n.470-355T=